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Mar 16, 2021 (publication date) through Nov 28, 2024
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Publication Name
World Journal of Clinical Cases
ISSN
2307-8960
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Zhang D, Sun JR, Xu J, Xing Y, Zheng M, Ye SD, Zhu J. 17α-hydroxylase/17,20 carbon chain lyase deficiency caused by p.Tyr329fs homozygous mutation: Three case reports . World J Clin Cases 2021; 9(8): 1923-1930 [PMID: 33748243 DOI: 10.12998/wjcc.v9.i8.1923] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v9/i8/1923.htm |
| Number | Citing Articles |
| 1 |
Jiaming Huang, Danli Zhou, Nan Dong, Chenzhao Ding, Yan Liu, Fangping Li. Clinical and Genetic Analysis of a Patient With Coexisting 17a-Hydroxylase/17,20-Lyase Deficiency and Moyamoya Disease. Frontiers in Genetics 2022; 13 doi: 10.3389/fgene.2022.845016
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| 2 |
Xu Sun, Yijun Wu, Lin Lu, Weibo Xia, Li Zhang, Shi Chen, Min Nie, Guangyao Zheng, Wan Su, Huijuan Zhu, Zhaolin Lu. Bone Microarchitecture and Volumetric Mineral Density Assessed by HR-pQCT in Patients with 21- and 17α-Hydroxylase Deficiency. Calcified Tissue International 2023; 113(5): 515 doi: 10.1007/s00223-023-01132-w
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| 3 |
Li Hui Han, Liang Wang, Xiu Yun Wu. 17 alpha‐hydroxylase deficiency: A case report of young Chinese woman with a rare gene mutation. Clinical Case Reports 2022; 10(7) doi: 10.1002/ccr3.6109
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| 4 |
Gamze Akkus. Two Cases with 17-alpha Hydroxylase Deficiency Misdiagnosed as Primary
Aldosteronism. Endocrine, Metabolic & Immune Disorders - Drug Targets 2023; 23(11): 1449 doi: 10.2174/1871530323666230407125523
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| 5 |
Min Yin, Jiaxin Yang, Qinjie Tian, Xinyue Zhang. Ovarian gonadoblastoma with dysgerminoma in a girl with 46,XX karyotype 17a-hydroxylase/17, 20-lyase deficiency: A case report and literature review. Frontiers in Endocrinology 2022; 13 doi: 10.3389/fendo.2022.989695
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